MKC8866
规格
Cas Number | 1338934-59-0 |
规格或纯度 | ≥97% |
纯度 | ≥97% |
包装 | 100mg 或 250mg 或 50mg 或 5mg 或 25mg 或 2mg |
产品信息
别名 | 7-羟基-6-甲氧基-4-甲基-3-(2-吗啉-2-氧乙基)-2-氧代-2H-苯并吡喃-8-醛 |
品牌 | 阿拉丁 |
溶解性 | Solubility (25°C) In vitro DMSO: 3 mg/mL (8.3 mM); Water: ˂1 mg/mL Ethanol: ˂1 mg/mL |
简短描述 | IRE1 抑制剂 |
英文简短描述 | IRE1 Inhibitors |
过滤标签 | IRE1,Cell Cycle/DNA Damage |
储存温度 | -20°C储存 |
运输条件 | 超低温冰袋运输 |
生化和生理学机理 | MKC8866(IRE1-IN-8866)是一种水杨醛类似物,是一种特异性 IRE1α RNase 抑制剂,在体外对人类 IRE1α 的 IC50 为 0.29u2009μM 。 |
英文描述 |
Information MKC8866 MKC8866 (IRE1-IN-8866), a salicylaldehyde analog, is a specific IRE1α RNase inhibitor with IC50 of 0.29 μM for human IRE1α in vitro. Targets hIRE1α (Cell-free assay) 0.29 μM In vitro MKC8866 is optimized and refined from a family of IRE1α-specific endoribonuclease inhibitors obtained from a chemical library screen. MKC8866 effectively represses IRE1α-mediated XBP1 splicing in PCa cells and has favorable pharmacokinetic and pharmacodynamic properties. In vivo MKC8866 is an IRE1α RNase-specific inhibitor molecule that displays significant therapeutic activity in various preclinical models of PCa in vivo. MKC8866 synergizes with clinical PCa drugs in vivo. Cell Research(from reference) Cell lines:human PCa cell lines LNCaP and 22Rv1, VCaP cell line, C4-2B cell line Concentrations:0.2-10 μM Incubation Time:0.25-24 h |